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Lamisil
Lamisil - 0067-6171-85 - (TERBINAFINE HYDROCHLORIDE)
Drug Information of Lamisil
| Product NDC: | 0067-6171 |
| Proprietary Name: | Lamisil |
| Non Proprietary Name: | TERBINAFINE HYDROCHLORIDE |
| Active Ingredient(s): | 10 mg/g & nbsp; TERBINAFINE HYDROCHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lamisil
| Product NDC: | 0067-6171 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020980 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050810 |
Package Information of Lamisil
| Package NDC: | 0067-6171-85 |
| Package Description: | 1 TUBE in 1 CARTON (0067-6171-85) > 24 g in 1 TUBE |
NDC Information of Lamisil
| NDC Code | 0067-6171-85 |
| Proprietary Name | Lamisil |
| Package Description | 1 TUBE in 1 CARTON (0067-6171-85) > 24 g in 1 TUBE |
| Product NDC | 0067-6171 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TERBINAFINE HYDROCHLORIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20050810 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | TERBINAFINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
